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Updated: Aug 24, 2026

Identifying Dysregulated Genes Induced by Kaposi's Sarcoma-associated Herpesvirus (KSHV)
Published on: September 14, 2010
Micronodular Kaposi's sarcoma - a new variant of classic-sporadic Kaposi's sarcoma
Werner Kempf1, Gieri Cathomas, Günter Burg
1Department of Dermatology, Institute for Clinical Pathology, University Hospital Zurich, Zurich, Switzerland. kempf@derm.unizh.ch
Abstract:
Kaposi's sarcoma (KS) in its classic-sporadic form is a rare vascular neoplasm affecting predominantly elderly men of Jewish or Mediterranean origin. Women are very rarely affected by KS. The tumor manifests itself most commonly with brownish macular or infiltrated oval lesions on the lower legs in both genders. Human herpesvirus 8 (HHV-8) has recently been demonstrated to be etiologically linked to KS. We report a 51-year-old HIV-seronegative Caucasian woman with an unusual, previously not described variant of KS which presented with small (3 mm in diameter) scattered firm red papules on her right arm. The histology with nodular spindle cell tumor expressing endothelial markers, the demonstration of serum antibodies against HHV-8 and the presence of viral nucleic acids in the lesional tissue proved the diagnosis of the nodular stage of KS. An indolent course characterized by clinically identical seasonal recurrences, even after surgical treatment and cryosurgery, was observed during the follow-up period of 9 years. We propose the term 'micronodular KS' for this unusual clinical variant of KS mimicking capillary hemangioma.
Insights
This study describes a rare variant of Kaposi
Area of Science:
- Oncology
- Dermatology
- Virology
Background:
- Kaposi's sarcoma (KS) is a rare vascular neoplasm, typically affecting elderly men, and is etiologically linked to Human Herpesvirus 8 (HHV-8).
- Classic-sporadic KS predominantly affects men of Jewish or Mediterranean origin, presenting as brownish lesions on the lower legs.
- KS is rarely observed in women and typically presents differently than in men.
Observation:
- A 51-year-old, HIV-seronegative Caucasian woman presented with an unusual variant of KS.
- The variant manifested as small, scattered, firm red papules on her right arm, differing from typical KS presentations.
- Histology confirmed a nodular spindle cell tumor expressing endothelial markers, with evidence of HHV-8 antibodies and viral nucleic acids.
Findings:
- The diagnosis of the nodular stage of KS was confirmed through histological and serological markers.
- The patient experienced an indolent course with seasonal recurrences over 9 years, despite surgical and cryosurgical treatments.
- This presentation represents a previously undescribed clinical variant of KS.
Implications:
- The term 'micronodular KS' is proposed for this distinct clinical variant.
- This variant mimics capillary hemangioma, highlighting the diverse clinical spectrum of KS.
- Understanding this variant is crucial for accurate diagnosis and management of rare KS cases.
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